Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Kengo Kosaka"'
Autor:
Shuhei Sekii, Kayoko Tsujino, Kengo Kosaka, Satoshi Yamaguchi, Hikaru Kubota, Yoko Matsumoto, Yosuke Ota, Ryohei Sasaki, Toshinori Soejima
Publikováno v:
Journal of Contemporary Brachytherapy, Vol 10, Iss 5, Pp 470-477 (2018)
Externí odkaz:
https://doaj.org/article/40bd396cfe7241d184a94877395ac1c6
Autor:
Yoshiki Takei, Kengo Kosaka
Publikováno v:
Japanese Journal of Radiological Technology. 77:212-219
Autor:
Kengo Kosaka, Eiji Matsuura, Shin Ichiro Mori, Shiroh Miura, Ryuta Fujioka, Hirotomo Saitsu, Ken Yamamoto, Kazuhito Noda, Fujio Umehara, Tomofumi Shimojo, Hiroki Shibata, Toru Iwaki
Publikováno v:
Journal of Human Genetics. 65:717-725
In 2008, we reported a clinically and genetically new type of autosomal dominant disorder of motor and sensory neuropathy with proximal dominancy in the lower extremities, urinary disturbance, and paroxysmal dry cough. To identify the nucleotide vari
Autor:
Kenji Uemoto, Kengo Kosaka
Publikováno v:
Japanese Journal of Radiological Technology. 76:1067-1073
Autor:
Kayoko Tsujino, Yosuke Ota, Kengo Kosaka, Shuhei Sekii, Nor Shazrina Sulaiman, Ryohei Sasaki, Yoko Matsumoto, Shuichiro Miyazaki, Satoshi Yamaguchi, Toshinori Soejima, Hikaru Kubota
Publikováno v:
Journal of Radiation Research
Our observational study aimed to verify the safety of our original titanium fiducial markers in gynecological cancer by using a simple insertion method. We prospectively evaluated the safety in patients with gynecological cancer who had undergone our
Autor:
Akihiro Nagano, Shiroh Miura, Hiroaki Ohishi, Takuya Morikawa, Motoko Unoki, Kengo Kosaka, Hiroyuki Sasaki, Kosei Moriyama, Motonao Nakao, Takeshi Bamba, Yoshihiro Izumi, Masatomo Takahashi, Itsuki Taniguchi, Tomofumi Shimojo, Ryuta Fujioka, Hiroki Shibata
Publikováno v:
Bioscience Reports
We have previously reported a novel homozygous 4-bp deletion in DDHD1 as the responsible variant for spastic paraplegia type 28 (SPG28; OMIM#609340). The variant causes a frameshift, resulting in a functionally null allele in the patient. DDHD1 encod
Autor:
Takayuki Taniwaki, Masaya Harada, Kengo Kosaka, Hiroki Shibata, Takuo Nomura, Shuji Nagata, Takuya Morikawa, Tomofumi Shimojo, Ryuta Fujioka, Shiroh Miura
Publikováno v:
European journal of medical genetics. 62(12)
Distal hereditary motor neuropathies (dHMNs) comprise a group of clinically and genetically heterogeneous inherited lower motor neuron syndromes mainly characterized by a distal-predominant pattern of progressive muscle atrophy, weakness and hyporefl
Autor:
Azusa Irie, Shiroh Miura, Hiroki Shibata, Yusuke Uchiyama, Takayuki Taniwaki, Takuya Morikawa, Ryuta Fujioka, Tomofumi Shimojo, Kengo Kosaka
Publikováno v:
European journal of medical genetics. 62(3)
Spinocerebellar ataxia 27 (SCA27) is an autosomal dominant SCA caused by variants in the fibroblast growth factor 14 (FGF14) gene. We examined a Japanese SCA patient whose deceased father also suffered from SCA. The patient was a 63-year-old male. He
Autor:
Takuya Morikawa, Hiroaki Ohishi, Kengo Kosaka, Tomofumi Shimojo, Akihiro Nagano, Itsuki Taniguchi, Ryuta Fujioka, Kosei Moriyama, Motoko Unoki, Masatomo Takahashi, Motonao Nakao, Yoshihiro Izumi, Takeshi Bamba, Hiroyuki Sasaki, Shiroh Miura, Hiroki Shibata
Publikováno v:
Bioscience Reports; Feb2021, Vol. 41 Issue 2, p1-13, 13p
Autor:
Kengo Kosaka, Hiroki Shibata, Ryuta Fujioka, Shiroh Miura, Takuya Morikawa, Takayuki Taniwaki, Kazuhito Noda
Publikováno v:
European journal of medical genetics. 60(9)
Dominant intermediate Charcot-Marie-Tooth disease F (CMTDIF) is an autosomal dominant hereditary form of Charcot-Marie-Tooth disease (CMT) caused by variations in the guanine nucleotide-binding protein, subunit beta-4 gene (GNB4). We examined two Jap